Barker C J, Nilsson T, Kirk C J, Michell R H, Berggren P O
Centre for Clinical Research in Immunology and Signalling, University of Birmingham, Edgbaston, U.K.
Biochem J. 1994 Jan 15;297 ( Pt 2)(Pt 2):265-8. doi: 10.1042/bj2970265.
Changes in the cytoplasmic free Ca2+ concentration ([Ca2+]i) in stimulated cells are often oscillatory, but the mechanisms that drive these oscillations are still a matter of controversy: different models of the generation of these [Ca2+]i oscillations make different assumptions as to whether oscillations in Ins(1,4,5)P3 concentration are necessary for this process. We have looked for changes in inositol polyphosphate levels that might occur in suspensions of murine pancreatic beta-cells when these cells are induced to display synchronized oscillations in [Ca2+]i by the sequential addition of glucose, an alpha 2-adrenergic stimulus and extracellular Ca2+. The intracellular level of Ins(1,4,5)P3 oscillated in a manner approximately in synchrony with changes in [Ca2+]i. Oscillations in the levels of Ins(1,4,5)P3 metabolites [Ins(1,3,4)P3 and inositol bisphosphates] were slightly delayed relative to the Ins(1,4,5)P3 oscillations, and the concentration of Ins(1,3,4,5,6)P5 remained approximately constant during the [Ca2+]i oscillations. These results demonstrate that [Ins(1,4,5)P3] and [Ca2+]i oscillate in synchrony in at least one type of cell. Whether such oscillations in intracellular [Ins(1,4,5)P3] provide a primary driving force for [Ca2+]i oscillations either in beta-cells or in other stimulated cells remains to be determined. Even if they do not, the [Ins(1,4,5)P3] oscillations will at least provide an amplifying influence on the [Ca2+]i changes.
受刺激细胞中细胞质游离钙离子浓度([Ca2+]i)的变化通常是振荡性的,但驱动这些振荡的机制仍存在争议:关于这些[Ca2+]i振荡的产生,不同模型对于肌醇-1,4,5-三磷酸(Ins(1,4,5)P3)浓度的振荡在此过程中是否必要做出了不同假设。我们研究了小鼠胰腺β细胞悬液中,当通过依次添加葡萄糖、α2-肾上腺素能刺激物和细胞外钙离子诱导这些细胞呈现[Ca2+]i同步振荡时,肌醇多磷酸水平可能发生的变化。Ins(1,4,5)P3的细胞内水平以一种大致与[Ca2+]i变化同步的方式振荡。Ins(1,4,5)P3代谢物([Ins(1,3,4)P3和肌醇二磷酸])的水平振荡相对于Ins(1,4,5)P3振荡略有延迟,并且在[Ca2+]i振荡期间,Ins(1,3,4,5,6)P5的浓度大致保持恒定。这些结果表明,[Ins(1,4,5)P3]和[Ca2+]i在至少一种类型的细胞中同步振荡。细胞内[Ins(1,4,5)P3]的这种振荡是否为β细胞或其他受刺激细胞中的[Ca2+]i振荡提供主要驱动力仍有待确定。即使它们不是主要驱动力,[Ins(1,4,5)P3]振荡至少会对[Ca2+]i变化产生放大作用。